Sponheim S, Skraastad Ø, Helseth E, Due-Tønnesen B, Aamodt G, Breivik H
Department of Anesthesiology, Rikshospitalet University Hospital, Oslo, Norway.
Acta Anaesthesiol Scand. 2003 Sep;47(8):932-8. doi: 10.1034/j.1399-6576.2003.00199.x.
Isoflurane has been a commonly used agent for neuroanesthesia, but newer agents, sevoflurane and desflurane, have a quicker onset and shorter emergence from anesthesia and are increasingly preferred for general pediatric anesthesia. But their effects on intracranial pressure (ICP) and cerebral perfusion pressure (CPP), especially in pediatric patients with already increased ICP, have not been well documented.
We studied 36 children scheduled for elective implantation of an intraparenchymal pressure device for 24 h monitoring for suspected elevated ICP. After a standardized intravenous anesthesia, the patients were moderately hyperventilated with 60% nitrous oxide (N2O) in oxygen. The patients were then randomized to receive 0.5 and 1.0 MAC of isoflurane (Group I, n = 12), sevoflurane (Group S, n = 12) or desflurane (Group D, n = 12) in 60% N2O in oxygen. Respiratory and hemodynamic variables, ICP and CPP were recorded at baseline and after exposure to a target level of test drug for 10 min or until CPP fell below 30 mmHg (recommended lower ICP level is 25 mmHg in neonates, rising to 40 mmHg in toddlers).
When comparing baseline values with values at 1.0 MAC, mean arterial pressure (MAP) decreased (P < 0.001) in all groups, with no differences between the groups. ICP increased (P < 0.001) with all agents, mean +2, +5, and +6 mmHg in Group I, S and D, respectively, with no differences between the groups. Regression analyzes found no relationship between baseline ICP and the increases in ICP from baseline to 1.0 MAC for isoflurane or sevoflurane. However, increased baseline ICP tended to cause a higher ICP increase with 1.0 MAC desflurane; regression coefficient +0.759 (P = 0.077). The difference between regression coefficients for Group I and Group D were not significant (P = 0.055). CPP (MAP-ICP) decreased (P < 0.001) in all groups, mean -18, -14 and -17 mmHg in Group I, S and D, respectively, with no significant difference between the groups.
0.5 and 1.0 MAC isoflurane, sevoflurane and desflurane in N2O all increased ICP and reduced MAP and CPP in a dose-dependent and clinically similar manner. There were no baseline dependent increases in ICP from 0 to 1.0 MAC with isoflurane or sevoflurane, but ICP increased somewhat more, although statistically insignificant, with higher baseline values in patients given desflurane. The effect of MAP on CPP is 3-4 times higher than the effect of the increases in ICP on CPP and this makes MAP the most important factor in preserving CPP. In children with known increased ICP, intravenous anesthesia may be safer. However, maintaining MAP remains the most important determinant of a safe CPP.
异氟烷一直是神经麻醉中常用的药物,但新型药物七氟烷和地氟烷起效更快、麻醉苏醒时间更短,在小儿全身麻醉中越来越受青睐。但它们对颅内压(ICP)和脑灌注压(CPP)的影响,尤其是对已有ICP升高的小儿患者的影响,尚未有充分的文献记载。
我们研究了36例计划择期植入脑实质内压力监测装置以监测疑似升高的ICP达24小时的儿童。在标准化静脉麻醉后,患者用60%氧化亚氮(N₂O)与氧气进行适度过度通气。然后将患者随机分为三组,分别在60% N₂O与氧气中接受0.5和1.0 MAC的异氟烷(I组,n = 12)、七氟烷(S组,n = 12)或地氟烷(D组,n = 12)。在基线时以及暴露于目标水平的试验药物10分钟后或直至CPP降至30 mmHg以下(推荐的新生儿较低ICP水平为25 mmHg,幼儿升至40 mmHg),记录呼吸和血流动力学变量、ICP和CPP。
将基线值与1.0 MAC时的值进行比较时,所有组的平均动脉压(MAP)均下降(P < 0.001),组间无差异。所有药物均使ICP升高(P < 0.001),I组、S组和D组分别平均升高+2、+5和+6 mmHg,组间无差异。回归分析发现,基线ICP与异氟烷或七氟烷从基线到1.0 MAC时ICP的升高之间无相关性。然而,基线ICP升高往往会使1.0 MAC地氟烷导致更高的ICP升高;回归系数为+0.759(P = 0.077)。I组和D组回归系数之间的差异不显著(P = 0.055)。所有组的CPP(MAP - ICP)均下降(P < 0.001),I组、S组和D组分别平均下降-18、-14和-17 mmHg,组间无显著差异。
N₂O中的0.5和1.0 MAC异氟烷、七氟烷和地氟烷均以剂量依赖性且临床上相似的方式升高ICP并降低MAP和CPP。异氟烷或七氟烷从0到1.0 MAC时ICP无基线依赖性升高,但地氟烷给药患者基线值较高时,ICP升高幅度虽无统计学意义但稍大。MAP对CPP的影响比ICP升高对CPP的影响高3 - 4倍,这使得MAP成为维持CPP的最重要因素。在已知ICP升高的儿童中,静脉麻醉可能更安全。然而,维持MAP仍然是安全CPP的最重要决定因素。